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Journal Abstract Search

221 related items for PubMed ID: 10398231

  • 1. X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3.
    Siderius LE, Hamel BC, van Bokhoven H, de Jager F, van den Helm B, Kremer H, Heineman-de Boer JA, Ropers HH, Mariman EC.
    Am J Med Genet; 1999 Jul 30; 85(3):216-20. PubMed ID: 10398231
    [Abstract] [Full Text] [Related]

  • 2. Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: clinical and psychometric data and results of linkage analysis.
    Hamel BC, Smits AP, van den Helm B, Smeets DF, Knoers NV, van Roosmalen T, Thoonen GH, Assman-Hulsmans CF, Ropers HH, Mariman EC, Kremer H.
    Am J Med Genet; 1999 Jul 30; 85(3):290-304. PubMed ID: 10398246
    [Abstract] [Full Text] [Related]

  • 3. Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1.
    Claes S, Volcke P, Devriendt K, Holvoet M, Raeymaekers P, Cassiman JJ, Fryns JP.
    Am J Med Genet; 1999 Jul 30; 85(3):283-7. PubMed ID: 10398244
    [Abstract] [Full Text] [Related]

  • 4. Narrowing the map of a gene (MRXS9) for X-linked mental retardation, microcephaly, and variably short stature at Xq12-q21.31.
    Shrimpton AE, Braddock BR, Hoo JJ.
    Am J Med Genet; 2000 May 15; 92(2):155-6. PubMed ID: 10797443
    [No Abstract] [Full Text] [Related]

  • 5. A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11.
    Deqaqi SC, N'Guessan M, Forner J, Sbiti A, Beldjord C, Chelly J, Sefiani A, Des Portes V.
    Ann Genet; 1998 May 15; 41(1):11-6. PubMed ID: 9599645
    [Abstract] [Full Text] [Related]

  • 6. Non-specific X-linked mental retardation: linkage analysis in MRX2 and MRX4 families revisited.
    Hu LJ, Blumenfeld-Heyberger S, Hanauer A, Weissenbach J, Mandel JL.
    Am J Med Genet; 1994 Jul 15; 51(4):569-74. PubMed ID: 7943041
    [Abstract] [Full Text] [Related]

  • 7. A new X linked neurodegenerative syndrome with mental retardation, blindness, convulsions, spasticity, mild hypomyelination, and early death maps to the pericentromeric region.
    Hamel BC, Wesseling P, Renier WO, van den Helm B, Ropers HH, Kremer H, Mariman EC.
    J Med Genet; 1999 Feb 15; 36(2):140-3. PubMed ID: 10051014
    [Abstract] [Full Text] [Related]

  • 8. Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33).
    Holinski-Feder E, Golla A, Rost I, Seidel H, Rittinger O, Meindl A.
    Am J Med Genet; 1996 Jul 12; 64(1):125-30. PubMed ID: 8826462
    [Abstract] [Full Text] [Related]

  • 9. The localization of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1X.
    Stanier P, Forbes SA, Arnason A, Bjornsson A, Sveinbjornsdottir E, Williamson R, Moore G.
    Genomics; 1993 Sep 12; 17(3):549-55. PubMed ID: 8244369
    [Abstract] [Full Text] [Related]

  • 10. Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50).
    Claes S, Vogels A, Holvoet M, Devriendt K, Raeymaekers P, Cassiman JJ, Fryns JP.
    Am J Med Genet; 1997 Dec 31; 73(4):474-9. PubMed ID: 9415477
    [Abstract] [Full Text] [Related]

  • 11. Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation.
    Gedeon AK, Glass IA, Connor JM, Mulley JC.
    Am J Med Genet; 1996 Jul 12; 64(1):121-4. PubMed ID: 8826461
    [Abstract] [Full Text] [Related]

  • 12. Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?
    Passos-Bueno MR, Byth BC, Rosenberg S, Takata RI, Bakker E, Beggs AH, Pavanello RC, Vainzof M, Davies KE, Zatz M.
    Am J Med Genet; 1993 Apr 15; 46(2):172-5. PubMed ID: 8484404
    [Abstract] [Full Text] [Related]

  • 13. A gene for nonspecific X-linked mental retardation (MRX41) is located in the distal segment of Xq28.
    Hamel BC, Kremer H, Wesby-van Swaay E, van den Helm B, Smits AP, Oostra BA, Ropers HH, Mariman EC.
    Am J Med Genet; 1996 Jul 12; 64(1):131-3. PubMed ID: 8826463
    [Abstract] [Full Text] [Related]

  • 14. Localization of a gene for X-linked nonspecific mental retardation (MRX24) in Xp22.2-p22.3.
    Martínez F, Gal A, Palau F, Prieto F.
    Am J Med Genet; 1995 Jan 30; 55(3):387-90. PubMed ID: 7726242
    [Abstract] [Full Text] [Related]

  • 15. Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait.
    Houdayer C, Soupre V, Rosenberg-Bourgin M, Martinez H, Tredano M, Feldmann D, Feingold J, Aymard P, Munnich A, Le Bouc Y, Vazquez MP, Bahuau M.
    Ann Genet; 1999 Jan 30; 42(2):69-74. PubMed ID: 10434119
    [Abstract] [Full Text] [Related]

  • 16. Pericentromeric genes for non-specific X-linked mental retardation (MRX).
    Gedeon A, Kerr B, Mulley J, Turner G.
    Am J Med Genet; 1994 Jul 15; 51(4):553-64. PubMed ID: 7943039
    [Abstract] [Full Text] [Related]

  • 17. Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28.
    Villard L, des Portes V, Levy N, Louboutin JP, Recan D, Coquet M, Chabrol B, Figarella-Branger D, Chelly J, Pellissier JF, Fontes M.
    Eur J Hum Genet; 2000 Feb 15; 8(2):125-9. PubMed ID: 10757644
    [Abstract] [Full Text] [Related]

  • 18. X-linked nonspecific mental retardation (MRX16) mapping to distal Xq28: linkage study and neuropsychological data in a large family.
    Gendrot C, Ronce N, Raynaud M, Ayrault AD, Dourlens J, Castelnau P, Muh JP, Chelly J, Moraine C.
    Am J Med Genet; 1999 Apr 23; 83(5):411-8. PubMed ID: 10232754
    [Abstract] [Full Text] [Related]

  • 19. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.
    Hamel BC, Mariman EC, van Beersum SE, Schoonbrood-Lenssen AM, Ropers HH.
    Am J Med Genet; 1994 Jul 15; 51(4):591-7. PubMed ID: 7943045
    [Abstract] [Full Text] [Related]

  • 20. Short stature, mental retardation, eye anomalies, and cleft lip/palate.
    Richieri-Costa A, Guion-Almeida ML.
    Am J Med Genet; 1992 Feb 15; 42(4):449-52. PubMed ID: 1609826
    [Abstract] [Full Text] [Related]

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